Dipeptide Boronic Acid Inhibitors of Dipeptidyl Peptidase IV: Determinants of Potency and in Vivo Efficacy and Safety

Beth A. Connolly(Tufts University), David G. Sanford(Tufts University), Amrita K. Chiluwal(Tufts University), Sarah E. Healey(Tufts University), Diane E. Peters(Tufts University), Matthew T. DiMare(Tufts University), Wengen Wu(Tufts University), Yuxin Liu(Tufts University), Hlaing Maw(Tufts University), Yuhong Zhou(Tufts University), Youhua Li(Tufts University), Zhiping Jin(Tufts University), James L. Sudmeier(Tufts University), Jack H. Lai(Tufts University), William W. Bachovchin(Tufts University)
Journal of Medicinal Chemistry
September 11, 2008
Cited by 71Open Access
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Abstract

Dipeptidyl peptidase IV (DPP-IV; E.C. 3.4.14.5), a serine protease that degrades the incretin hormones GLP-1 and GIP, is now a validated target for the treatment of type 2 diabetes. Dipeptide boronic acids, among the first, and still among the most potent DPP-IV inhibitors known, suffer from a concern over their safety. Here we evaluate the potency, in vivo efficacy, and safety of a selected set of these inhibitors. The adverse effects induced by boronic acid-based DPP-IV inhibitors are essentially limited to what has been observed previously for non-boronic acid inhibitors and attributed to cross-reactivity with DPP8/9. While consistent with the DPP8/9 hypothesis, they are also consistent with cross-reactivity with some other intracellular target. The results further show that the potency of simple dipeptide boronic acid-based inhibitors can be combined with selectivity against DPP8/9 in vivo to produce agents with a relatively wide therapeutic index (>500) in rodents.


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